Assessment of Endometrial and Sub-endometrial Vascularity Before and After PRP Infusion in Frozen Embryo Transfer Cycles

Sponsor
Hatem AbuHashim (Other)
Overall Status
Unknown status
CT.gov ID
NCT04247204
Collaborator
(none)
30
1
7.9

Study Details

Study Description

Brief Summary

A good quality embryo and receptive endometrium are important aspects in achieving optimal outcomes in assisted reproductive treatment (ART). Endometrial thickness is an important marker of uterine receptivity. A thin endometrium defined by an endometrial thickness ≤7mm was reported as a poor factor associated with significantly lower implantation and pregnancy rates as well as a higher risk of miscarriage.

Nowadays, platelet-rich plasma (PRP) intrauterine infusion is a promising approach for the treatment of refractory thin endometrium in patients undergoing frozen-thawed embryo transfer. This is based on its ability to stimulate proliferation and angiogenesis with a large number of growth factors and cytokines i.e. the endometrium becomes thicker, with higher vascularity. PRP is easily prepared from an autologous blood sample that eliminates the risk of immunological reactions and transmission infections at low cost.

Endometrial blood flow is another important marker reflective of uterine receptivity. Although publications are increasing concerning the efficacy of PRP intrauterine infusion on endometrial expansion and proliferation in frozen-thawed embryo transfer cycles, yet its angiogenetic effects have not been evaluated so far in either thin endometrium or normal endometrium thickness.

Our study aims to evaluate endometrial and sub-endometrial vasculature patterns before and after PRP infusion in frozen-thawed embryo transfer cycles with normal endometrium thickness.

Condition or Disease Intervention/Treatment Phase
  • Biological: Platelet-rich plasma intrauterine infusion
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
3D Power Doppler Ultrasound Assessment of Endometrial and Sub-endometrial Vascularity Before and After PRP Infusion in Frozen-thawed Embryo Transfer Cycles: a Pilot Study.
Anticipated Study Start Date :
Feb 8, 2020
Anticipated Primary Completion Date :
Aug 31, 2020
Anticipated Study Completion Date :
Oct 5, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Platelet-rich plasma (PRP) intrauterine infusion

Biological: Platelet-rich plasma intrauterine infusion
For all women, basic transvaginal sonography will be done in the 2nd day of frozen embryo transfer (FET) cycle and they will receive standard hormone replacement therapy (HRT) in the form of estradiol valerate tablets (white tablets of Cyclo-Progynova; Bayer Schering Pharma AG, Germany) at a dose of 4mg for 7 days then 6mg for 6 days. Endometrial assessment will be done on day 15 of FET cycle. Those with endometrial thickness between 8-14 mm will be evaluated for endometrial and sub-endometrial vasculature pattern by 3D power Doppler analysis. Then 1 ml of PRP (prepared from autologous blood) will be infused in the uterine cavity and vaginal progesterone 400 mg twice daily will be prescribed for 3 days. Subsequently, D3 embryos will be transferred. Endometrial, sub-endometrial and uterine arterial vascularity pattern will be re-evaluated on the day of ET. Both estradiol valerate tablets and vaginal progesterone will be continued up to 12th week of gestation in case of pregnancy.

Outcome Measures

Primary Outcome Measures

  1. Vascularization index of the endometrial region [Day 15 to 18 of the frozen embryo transfer cycle]

    Vascularization index of the endometrial region will be measured by a researcher using the built-in VOCAL (Virtual Organ Computer-Aided Analysis) software for 3D power Doppler analysis.

Secondary Outcome Measures

  1. Flow index of the endometrial region [Day 15 to 18 of the frozen embryo transfer cycle]

    Flow index of the endometrial region will be measured by a researcher using the built-in VOCAL (Virtual Organ Computer-Aided Analysis) software for 3D power Doppler analysis

  2. Vascularization flow index of the endometrial region [Day 15 to 18 of the frozen embryo transfer cycle]

    Vascularization flow index of the endometrial region will be measured by a researcher using the built-in VOCAL (Virtual Organ Computer-Aided Analysis) software for 3D power Doppler analysis

  3. Vascularization index of the sub-endometrial region [Day 15 to 18 of the frozen embryo transfer cycle]

    Vascularization flow index of the sub-endometrial region will be measured by a researcher using the built-in VOCAL (Virtual Organ Computer-Aided Analysis) software for 3D power Doppler analysis

  4. Flow index of the sub-endometrial region [Day 15 to 18 of the frozen embryo transfer cycle]

    Flow index of the sub-endometrial region will be measured by a researcher using the built-in VOCAL (Virtual Organ Computer-Aided Analysis) software for 3D power Doppler analysis

  5. Vascularization flow index of the sub-endometrial region [Day 15 to 18 of the frozen embryo transfer cycle]

    Vascularization flow index of the sub-endometrial region will be measured by a researcher using the built-in VOCAL (Virtual Organ Computer-Aided Analysis) software for 3D power Doppler analysis

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 35 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Subfertile women undergoing frozen-thawed embryo transfer with at least previously failed one ICSI cycle.

  • Age between 20-35 years.

  • Women with endometrium thickness between 8-14 mm on D15 of the frozen embryo transfer cycle

Exclusion Criteria:
  • Women with a thin endometrium (≤ 7 mm) on day 15 of the cycle.

  • Women with known hematological or immunological disorders

  • Women with uncontrolled endocrine or other medical conditions, such as hyperprolactinemia or thyroid diseases.

  • Women with uterine abnormalities e.g. Asherman syndrome, myomas, uterine septum, bicornuate uterus.

  • Women who refuse to participate in the study.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Hatem AbuHashim

Investigators

  • Study Chair: Hatem Abu Hashim, MD. FRCOG. PhD, Faculty of Medicine, Mansoura University
  • Principal Investigator: Mohamed Taman, MD, Faculty of Medicine, Mansoura University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Hatem AbuHashim, Professor, Mansoura University
ClinicalTrials.gov Identifier:
NCT04247204
Other Study ID Numbers:
  • R.20.01.711
First Posted:
Jan 29, 2020
Last Update Posted:
Jan 29, 2020
Last Verified:
Jan 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jan 29, 2020